Pigmented neoplasms of the peripheral nervous system are uncommon. Such lesions, while well documented in the para‐axial region, are infrequently encountered in more peripheral extra‐axial sites. The authors present a case of a melanocytic schwannoma arising in the gastric antrum of a 51‐yearold woman. Ultrastructural features attesting to the nerve sheath origin of the neoplasm included the presence of a well‐developed basal lamina, complex infoldings of the plasma membrane, and intercellular bundles of long spaced collagen (“Luse bodies”). Premelanosomes and melanosomes in all stages of development were identified within the cytoplasm of many of the neoplastic cells, providing morphologic support for a close relationship between Schwann cells and melanocytes. Immunoperoxidase studies with S‐100 protein disclosed intense cytoplasmic staining throughout the tumor. The S‐100 protein antigen has been documented in both nerve sheath elements and melanocytes; this shared antigenicity lends further support to the close relationship between melanocytic and schwannian elements suggested by ultrastructural observations. Additional immunoperoxidase studies employing antibody to glial fibrillary acidic protein revealed focal cytoplasmic staining, an uncommon phenomenon in peripheral nerve sheath neoplasms. A review of the literature failed to provide any previous well documented cases of melanocytic schwannoma of the stomach. The patient was treated with en bloc resection of the tumor and gastric antrum, and was free of evidence of recurrent or metastatic disease 22 months postoperatively. Theories regarding the histogenesis of pigmented nerve sheath neoplasms and prognostic implications are discussed, based on experience with this and previously reported pigmented nerve sheath tumors.
|Original language||English (US)|
|Number of pages||10|
|State||Published - Oct 15 1983|